Every two years, researchers from around the world gather at the international CAA (Cerebral Amyloid Angiopathy) conference. The Dutch DCAA patient association usually sends two representatives to learn about the latest research, network with researchers and physicians, and voice the perspectives of families affected by Dutch-type CAA. This October, we met in Munich. Since the conference was "close to home," as the patient association, we had extra room in our budget (aka our government subsidy), allowing a larger part of our board to attend. This year, Maike, Koos, Janny, Martina, Nicole, and Sanne were all present.
The conference was intens, interesting and exciting as always. Sanne wrote a summary for you, read it here.